FUKUDA DENSHI MODEL SPIROSIFT 3000— 510(k) K900391
Substantially EquivalentFukuda Denshi USA, Inc.
FDA 510(k) clearance K900391 for FUKUDA DENSHI MODEL SPIROSIFT 3000, Substantially Equivalent on 1990-04-10. Applicant: Fukuda Denshi USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Fukuda Denshi USA, Inc.
- Product code
- Code BZG
- Device class
- Class 2
- Regulation
- 21 CFR 868.1840
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Redmond, WA, US
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